CATHe: detection of remote homologues for CATH superfamilies using embeddings from protein language models

Author:

Nallapareddy Vamsi1ORCID,Bordin Nicola1ORCID,Sillitoe Ian1ORCID,Heinzinger Michael23ORCID,Littmann Maria23ORCID,Waman Vaishali P1,Sen Neeladri1ORCID,Rost Burkhard2345,Orengo Christine1

Affiliation:

1. Institute of Structural and Molecular Biology, University College London , London WC1E 6BT, UK

2. Department of Informatics , Bioinformatics and Computational Biology—i12 , , Garching/Munich 85748, Germany

3. Technical University of Munich (TUM) , Bioinformatics and Computational Biology—i12 , , Garching/Munich 85748, Germany

4. Institute for Advanced Study (TUM-IAS) , Garching/Munich 85748, Germany

5. TUM School of Life Sciences Weihenstephan (WZW) 85354, Germany

Abstract

AbstractMotivationCATH is a protein domain classification resource that exploits an automated workflow of structure and sequence comparison alongside expert manual curation to construct a hierarchical classification of evolutionary and structural relationships. The aim of this study was to develop algorithms for detecting remote homologues missed by state-of-the-art hidden Markov model (HMM)-based approaches. The method developed (CATHe) combines a neural network with sequence representations obtained from protein language models. It was assessed using a dataset of remote homologues having less than 20% sequence identity to any domain in the training set.ResultsThe CATHe models trained on 1773 largest and 50 largest CATH superfamilies had an accuracy of 85.6 ± 0.4% and 98.2 ± 0.3%, respectively. As a further test of the power of CATHe to detect more remote homologues missed by HMMs derived from CATH domains, we used a dataset consisting of protein domains that had annotations in Pfam, but not in CATH. By using highly reliable CATHe predictions (expected error rate <0.5%), we were able to provide CATH annotations for 4.62 million Pfam domains. For a subset of these domains from Homo sapiens, we structurally validated 90.86% of the predictions by comparing their corresponding AlphaFold2 structures with structures from the CATH superfamilies to which they were assigned.Availability and implementationThe code for the developed models is available on https://github.com/vam-sin/CATHe, and the datasets developed in this study can be accessed on https://zenodo.org/record/6327572.Supplementary informationSupplementary data are available at Bioinformatics online.

Funder

BBSRC

Software Campus 2.0

German Ministry for Research and Education

Deutsche Forschungsgemeinschaft

Bavarian Ministry of Education

Publisher

Oxford University Press (OUP)

Subject

Computational Mathematics,Computational Theory and Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Statistics and Probability

Reference45 articles.

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